Linked Data
dbSNP Id:
rs577850735
gnomAD v2:
22-42538408-T-G
gnomAD v3:
22-42142398-T-G
gnomAD v4:
22-42142398-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42142398T>G , CM000684.2:g.42142398T>G | GRCh38 |
| NC_000022.10:g.42538408T>G , CM000684.1:g.42538408T>G | GRCh37 |
| NC_000022.9:g.40868352T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651010.1:n.2620+81A>C | ||
| ENST00000358097.8:c.667+81A>C | ENSP00000445124.1:n.667+81A>C | |
| ENST00000433992.2:c.667+81A>C | ENSP00000439604.1:n.667+81A>C | |
| ENST00000610593.4:n.752+81A>C | ||
| ENST00000612115.1:c.666+81A>C | ENSP00000484065.1:n.666+81A>C | |
| ENST00000614967.4:c.513+81A>C | ENSP00000481168.1:n.513+81A>C | |
| NR_002570.3:n.778+81A>C | ||
| NM_001348386.2:c.666+81A>C | NP_001335315.1:n.666+81A>C | |
| NR_002570.5:n.686+81A>C | ||
| NR_145674.2:n.686+81A>C | ||
| NM_001348386.3:c.666+81A>C | NP_001335315.1:n.666+81A>C | |
| NR_002570.6:n.686+81A>C | ||
| NR_145674.3:n.686+81A>C |